ライフサイエンスコーパス: microcontact printing

1 aphy or via selective growth with the aid of microcontact printing.

2 n of cross-linked polymer thin-films through microcontact printing.

3 ently attaching and patterning a dye through microcontact printing.

4 ly onto self-assembled monolayer (SAM) using microcontact printing.

5 chlorosilane (OTS) monolayer patterned using microcontact printing.

6 ergy surfaces by a water-assisted variant of microcontact printing.

7 zed on azide-modified glass substrates using microcontact printing and a strain-promoted azide-alkyne

8 in chain organization between SAMs formed by microcontact printing and by solution deposition are als

9 rminated monolayers on gold surfaces and use microcontact printing and Dip-Pen Nanolithography (DPN)

10 Here, we use microcontact printing and microfabricated arrays of elas

11 d based on experimentally simple techniques--microcontact printing and micromolding in capillaries--t

12 In this study, we used microcontact printing and micropost arrays to control ce

13 Using samples prepared by DPN, microcontact printing, and adsorption on macroscopic sub

14 lectric-field alignment and crystallization, microcontact printing, and selective metallization.

15 n (tires, gaskets, and seals), biomaterials, microcontact printing, and soft robotics.

16 In traditional microcontact printing, diffusion limits resolution of pa

17 Microcontact printing, followed by fluorescence microsco

18 microelectrodes, microlenses, and stamps for microcontact printing, following methods described previ

19 ly larger compared to the currently-employed microcontact printing for PEMs.

20 , including methods for (i) rubber stamping (microcontact printing) high-resolution ( approximately 1

21 rogress enabled by transport control in e.g. microcontact printing, inkjet printing, dip-pen nanolith

22 printing with microfluidic patterning, where microcontact printing is employed for silanization using

23 EMs were created by ionic interactions using microcontact printing (microCP) technique.

24 face, we use techniques of soft lithography (microcontact printing, microfluidics, and patterning thr

25 ing micro- and nanodeposition tools, such as microcontact printing (muCP) and dip-pen nanolithography

26 e involves repeated surface patterning using microcontact printing (muCP) of initiator-terminated thi

27 tudy was conducted to investigate the use of microcontact printing (muCP) to direct cultured or expla

28 variety of experimental techniques including microcontact printing (muCP), surface plasmon resonance

29 monly used soft lithographic techniques: (i) microcontact printing of alkanethiols and proteins on go

30 Microarrays were fabricated by microcontact printing of BSA-PBA in line patterns (10 x

31 By microcontact printing of culture surfaces, we forced the

32 te pretreatment, and stamp contact times--on microcontact printing of m-dPEG acid molecules onto PEM

33 ts by geometrically inducing defects through microcontact printing of patterned monolayers.

34 M-1, created by combining multiple rounds of microcontact printing on a single surface.

35 Alkane thiols were patterned via microcontact printing on gold, and their effects on the

36 Furthermore, normalizing cell shape via microcontact printing on self-assembled monolayers enabl

37 d onto the substrate by optical lithography, microcontact printing or vapour deposition.

38 Microcontact printing provides an alternative to previou

39 adherent cells attached to defined areas via microcontact printing show that size stiffening is limit

40 Using microcontact printing, small (200-microm diameter) hydro

41 most of the patterning techniques, including microcontact printing (soft lithography), photolithograp

42 lica substrates through the combination of a microcontact printing technique and fusion of lipid vesi

43 near ECM islands, which were created using a microcontact printing technique and were 1 microm wide a

44 In conjunction with microcontact printing, this biomimetically catalyzed enc

45 Using microcontact printing to achieve spatial control of DNA-

46 um from sheep valve endothelial cells, using microcontact printing to mimic the regions of isotropy a

47 We use microcontact printing to pattern pentafluorobenzyl phosp

48 tionalized with extracellular matrix through microcontact printing to promote cell adhesion.

49 The additive process uses microcontact printing to transfer the target pattern.

50 d chemistry, and printed by inkjet, pin, and microcontact printing (uCP).

51 Microcontact printing was employed to pattern rHIgM12 an

52 Microcontact printing was used to functionalize portions

53 Using these features together with microcontact printing, we demonstrate straightforward pa

54 Using protein microcontact printing, we show that platelets spread bey

55 This approach consists of coupling microcontact printing with microfluidic patterning, wher

56 obilized catalyst, the lateral resolution of microcontact printing would depend only on the length an